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98015-45-3

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98015-45-3 Usage

Description

2-tert-Butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2-diazaphosphorine (BEMP) is a phosphazene base with exceptional basicity and steric hindrance. It is approximately 2000 times more basic than DBU (1,8-diazabicyclo[5.4.0]undecene) and exhibits significant steric hindrance, making it a potent catalyst in various chemical reactions.

Uses

Used in Chemical Synthesis:
BEMP is used as a catalyst in the mild base-catalyzed nucleophilic ring-opening of N-sulfonyl aziridines. Its high basicity and steric hindrance enable efficient catalysis, leading to the formation of various chemical products.
Used in Polymer-Supported Catalysts:
BEMP supported on polystyrene (PS-BEMP) is employed as an efficient catalyst for the ring-opening of epoxides with phenols. The polymer-supported catalyst allows for easy separation and recyclability, enhancing the practicality of the catalytic process.
Used in Pharmaceutical Industry:
BEMP's unique properties make it a promising candidate for the development of new pharmaceutical compounds. Its ability to act as a potent catalyst in various chemical reactions can facilitate the synthesis of novel drug molecules with potential therapeutic applications.
Used in Material Science:
The high basicity and steric hindrance of BEMP can be utilized in the synthesis of new materials with unique properties. For example, it can be employed in the development of advanced polymers, catalysts, and other materials with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 98015-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,1 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 98015-45:
(7*9)+(6*8)+(5*0)+(4*1)+(3*5)+(2*4)+(1*5)=143
143 % 10 = 3
So 98015-45-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H31N4P/c1-8-17(9-2)18(14-13(3,4)5)15(6)11-10-12-16(18)7/h8-12H2,1-7H3

98015-45-3 Well-known Company Product Price

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  • Sigma-Aldrich

  • (20025)  2-tert-Butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2-diazaphosphorine  purum, ≥98.0% (GC)

  • 98015-45-3

  • 20025-1ML

  • 1,313.91CNY

  • Detail
  • Sigma-Aldrich

  • (20025)  2-tert-Butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2-diazaphosphorine  purum, ≥98.0% (GC)

  • 98015-45-3

  • 20025-5ML

  • 5,073.12CNY

  • Detail
  • Sigma-Aldrich

  • (20025)  2-tert-Butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2-diazaphosphorine  purum, ≥98.0% (GC)

  • 98015-45-3

  • 20025-25ML

  • 19,141.20CNY

  • Detail
  • Aldrich

  • (728411)  2-tert-Butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2-diazaphosphorinesolution  1 M in hexane, ≥97% (GC), 97% (GC)

  • 98015-45-3

  • 728411-25ML

  • 2,343.51CNY

  • Detail
  • Aldrich

  • (728411)  2-tert-Butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2-diazaphosphorinesolution  1 M in hexane, ≥97% (GC), 97% (GC)

  • 98015-45-3

  • 728411-100ML

  • 7,569.90CNY

  • Detail

98015-45-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tert-butylimino-N,N-diethyl-1,3-dimethyl-1,3,2λ<sup>5</sup>-diazaphosphinan-2-amine

1.2 Other means of identification

Product number -
Other names BEMP phosphazene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:98015-45-3 SDS

98015-45-3Relevant articles and documents

Reversible and robust CO2 capture by equimolar task-specific ionic liquid-superbase mixtures

Wang, Congmin,Mahurin, Shannon M.,Luo, Huimin,Baker, Gary A.,Li, Haoran,Dai, Sheng

scheme or table, p. 870 - 874 (2010/09/04)

Integrated sorption systems consisting of 1:1 mixtures of an alcohol-functionalized ionic liquid and a superbase were found to be effective for CO2 capture under atmospheric pressure, eliminating the use of volatile n-alkanols or water. Conversely, by using the current approach, there is no longer a requirement for maintaining scrupulously dry conditions. The effect of ionic liquid structure, choice of superbase, their relative ratios, the sorption temperature, and the reaction time on the absorption and release of CO2 were investigated. Our results demonstrate that (i) this integrated ionic liquid-superbase system is capable of rapid and reversible capture of nearly one mole of CO2 per mole of superbase, (ii) the captured CO2 can be readily released by either mild heating or bubbling with an insert gas (N2, Ar), and (iii) this novel CO 2 chemisorption platform can be recycled with minimal loss of activity. This efficient and fully reversible catch-and-release process using non-volatile, task-specific ionic liquids provides an excellent alternative to current CO2 capture technologies, which are based largely around volatile alkanols or alkylamines. Furthermore, our integrated ionic liquid-superbase system can be used as a novel medium for supported liquid membranes, for which they demonstrate both good selectivity and permeability in model CO2/N2 gas separations.

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